Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

12951–12975 of 27721

HighFDA (Devices)·Z-1687-2024·2024-05-01
Water bottles used in dental treatment devices recalled for disassembly risk
Electro Medical Systems is recalling water bottles used with AIRFLOW dental devices because certain bottle collars can disassemble under pressure during treatment or storage. No injuries have been reported.
Product
Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number: EG-121 Software Version: N/A Product Description: These bottles are sold empty and are filled by the user with water fort dental treatments. The bottle is pressurized on the device during use. Componen
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1637-2024·2024-05-01
Medical diagnostic test kits recalled due to misaligned results window
Quidel InflammaDry MMP-9 test kits are recalled because the test results window is misaligned. Positive results may be hidden from view, potentially causing false negative readings.
Product
QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-1631-2024·2024-05-01
Hip replacement acetabular shell recalled for excessive deburring
Howmedica Osteonics is recalling TRIDENTII PSL CLUSTER58F hip replacement acetabular shells due to excessive deburring. The manufacturing defect affects units distributed nationwide and internationally.
Product
TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1630-2024·2024-05-01
Hip prosthesis shells recalled for manufacturing deburring defect
Howmedica Osteonics Corp. is recalling TRIDENTII PSL CLUSTER52E hip prostheses with excessive deburring on the acetabular shell edge, which could affect implant stability. Three units were distributed nationwide and internationally.
Product
TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1607-2024·2024-05-01
Vanguard Knee System Tibial Bearing Recalled for Manufacturing Damage
Biomet is recalling the Vanguard Knee System AS Tibial Bearing (Model 189082) due to possible damage during manufacturing. Affected units were distributed worldwide including the United States.
Product
Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with protective packaging in the form of a polyurethane bag, and sealed closed (inner barrier). The inner barrier is then placed into a PETG tray and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0475-2024·2024-05-01
Minolira extended-release tablets recalled due to discontinued quality assurance program
EPI Health is recalling 5,664 bottles of minolira tablets because the manufacturer discontinued its quality assurance program. Affected lots include T2201700 and T2201701, distributed nationwide.
Product
minolira (minocycline hydrochloride) extended-release tablets, 135mg 30-count Bottle, Rx Only, Mfg by: Dr Reddy's Laboratories Limited, INDIA, Manufactured for: EPI Health, LLC, Charleston, SC 29403, NDC 71403-102-30.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1627-2024·2024-05-01
Hip Implant Acetabular Shell May Have Excessive Deburring Manufacturing Defect
Howmedica Osteonics Corp. is recalling TRIDENTII HEMI CLUSTER66H hip implants because the acetabular shell may have excessive deburring, creating a smooth surface on the edge of the shell.
Product
TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1629-2024·2024-05-01
Hip replacement acetabular shell recalled for excessive deburring
Howmedica Osteonics is recalling TRIDENTII PSL CLUSTER50D acetabular shells for hip replacements due to excessive deburring resulting in smooth edges on the shell.
Product
TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0590-2024·2024-05-01
Tissue Processor Recall: HistoCore PEGASUS May Produce Damaged Specimens
Leica is recalling 98 HistoCore PEGASUS automated tissue processors due to a protocol configuration error that can produce poorly processed or damaged biopsy specimens.
Product
Leica HistoCore PEGASUS (PROCESSOR, TISSUE, AUTOMATED)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1621-2024·2024-05-01
Hip implant acetabular shell manufacturing defect recall affects patients
Howmedica Osteonics Corp. is recalling TRIDENTII HEMI CLUSTER44B hip implants due to excessive deburring on the acetabular shell edge. The recalled lot was distributed nationwide and internationally.
Product
TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0473-2024·2024-05-01
Cloderm Cream Recalled for Manufacturer Quality Assurance Program Discontinuation
EPI Health is recalling Cloderm cream due to discontinuation of the manufacturer's quality assurance program. This may result in products that do not meet specifications for identity, strength, purity, or quality.
Product
Cloderm (clocortolone pivalate) Cream, 0.1%, Rx Only, For Topical Use Only, Net Wt 45g, Manufactured for: EPI Health, LLC, Charleston, SC 29403, NDC 71403-804-90
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V010000·2024-05-01
Chrysler Pacifica Electrical Short Circuit May Cause Engine Shutdown
Chrysler is recalling certain 2017-2023 Pacifica Plug-In Hybrid vehicles due to a wiring connector short circuit that may cause unexpected engine shutdown and loss of drive power.
Product
CHRYSLER — 2021 CHRYSLER PACIFICA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0472-2024·2024-05-01
Prescription Drug Recall: Diltiazem Extended-Release Capsules Fail Dissolution Test
Glenmark Pharmaceuticals is recalling 3,264 bottles of Diltiazem Hydrochloride Extended-Release Capsules nationwide due to failure to meet dissolution specifications. The affected lot may not release the medication properly in the body.
Product
DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·24212·2024-04-25
Crosman Icon Air Rifles Recalled Due to Unexpected Discharge Injury Hazard
Crosman is recalling about 2,500 Icon Air Rifles because an uncocked and loaded rifle can discharge unexpectedly if jolted or dropped, posing an injury hazard. One unintended discharge has been reported, though no injuries have occurred.
Product
Crosman Icon Air Rifles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24208·2024-04-25
Oregon Tool Recalls Log Splitters Due to Injury Hazards
Oregon Tool is recalling about 29,560 log splitters and cylinder kits because the hydraulic cylinder rod can separate from the piston, causing unexpected movement of the wedge that poses injury risks. No injuries have been reported.
Product
Oregon, PowerPro, Country Tuff, and Speeco branded log splitters and cylinder kits
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24211·2024-04-25
Kids' Bike Helmets Recalled for Failure to Meet Safety Standards
Chau River Sports Outdoors is recalling about 200 kids' bike helmets sold on Temu.com because they fail to meet federal safety requirements and may not protect children's heads in a crash.
Product
Kid's Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24210·2024-04-25
JAKKS Pacific Recalls Mario Kart 24V Ride-On Racer Cars Due to Crash Hazard
JAKKS Pacific is recalling certain Mario Kart 24V Ride-On Racer Cars because the acceleration pedal can become clogged with debris and stick, causing the vehicle to crash. The company has received 65 reports of clogged pedals, including 15 crashes with one minor injury.
Product
Mario Kart™ 24V Ride-On Racer Cars
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1160-2024·2024-04-24
Tejocote Root Dietary Supplement Recalled Due to Yellow Oleander
H&Natural is recalling tejocote root supplement due to the presence of yellow oleander and its components. The product was distributed exclusively through internet sales.
Product
H&NATURAL TEJOCOTE ROOT TWO PACK 180 PIECES, 6 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-1163-2024·2024-04-24
Brazil Seed Dietary Supplement Recalled for Yellow Oleander Contamination
HandNatural recalls H&Natural Brazil Seed supplement due to presence of yellow oleander and its components. The product was distributed via internet sales.
Product
H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOTTLE, 2 BLACK BOTTLES.
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1172-2024·2024-04-24
Brazil seed dietary supplement recalled for yellow oleander contamination
HandNatural's H&Natural Brazil Seed dietary supplement is being recalled due to the presence of yellow oleander, a toxic plant component. Distribution was exclusively through internet sales.
Product
H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, ORANGE BOTTLE.
Category
Drug
Distribution
0 states
SevereFDA (Devices)·Z-1502-2024·2024-04-24
Philips Trilogy EV300 Ventilator False Power Alarm Defect Recall
Philips is recalling 56,012 Trilogy EV300 ventilators due to a software defect that can trigger a false Battery Depleted or Loss of Power alarm despite adequate power, risking sudden loss of ventilation.
Product
Trilogy EV300, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1165-2024·2024-04-24
Brazil Seed Dietary Supplement Recalled for Yellow Oleander Contamination
H&NATURAL Brazil Seed supplement containing yellow oleander has been recalled by the FDA as a Class I health hazard. The product was distributed exclusively through internet sales.
Product
H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 YELLOW BOXES
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0442-2024·2024-04-24
Vancomycin Hydrochloride Oral Solution Recalled Nationwide for Superpotency Due to Overfilling
Amneal Pharmaceuticals is recalling Vancomycin Hydrochloride Oral Solution nationwide due to manufacturing overfilling causing superpotency with higher-than-labeled concentration. The FDA classified this as Class I.
Product
VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1520-2024·2024-04-24
SonarMed Airway Monitoring Sensor Fails to Detect Partial Obstruction
SonarMed Inc is recalling 690 units of the AW-S030 NEO SONARMED SENSOR because the sensor fails to detect partial airway obstruction. The devices were distributed across 20 US states.
Product
AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.
Category
Medical Device
Distribution
19 states
SevereFDA (Devices)·Z-1519-2024·2024-04-24
SonarMed 2.5mm Airway Sensor Recalled for Obstruction Detection Failure
SonarMed Inc is recalling the AW-S025 NEO SONARMED SENSOR 2.5MM airway monitoring device due to a malfunction that causes it to fail detecting partial obstruction, potentially preventing clinicians from identifying compromised airways.
Product
AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
Category
Medical Device
Distribution
19 states

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